RESUMO
The effects of benzene on the swimming activity of the crustacean Mysidopsis juniae were investigated. The swimming activity of M. juniae was observed after 1.3 and 6 h of exposure to 5, 10 15 and 20 ppm benzene in sea water (35 ñ 1 grade/00 S, 25 ñ 1 grade C). The mysids were observed with a pair of coupled to a camara lucida, and the swimming activity was measured in a Petri dish, corresponding to the distance (cm) covered by the animals in 1 min (N=150 animals). The swimming activity of mysids exposed to 20 ppm benzene decreased significantly after all three periods of exposure to values which were 80-90% smaller than the control value. On the other hand, after 6 h exposure to 5 ppm benzene, the swimming activity of the mysids was significantly higher, increasing by 87% in relation to the control (29.8 ñ 8.9 cm?min). Furthermore, a slight nonsignificant increase in swimming activity was also observed in mysids submitted to 5, 10, 15 and even 20 ppm benzene, as the period of exposure to the pollutant increased from 1 to 6 h. These results indicate that short-term exposure to sublethal benzene concentrations can affect the swimming activity of mysids. in these situations, mysid populations can be seriously damaged since alterations in swimming activity could lead to a reduction in food intake and to a marked increase in their susceptibility to predation by other organisms
Assuntos
Benzeno/efeitos adversos , Crustáceos , Natação , Poluição da ÁguaRESUMO
1. An in vitro bioassay for melanotropic peptide utilizing reflectance measurements of toad skin (Bufo ictericus ictericus) is described as an alternative to the commonly used Rana pipiens bioassay. 2. The toad skin bioassay is as sensitive to melanotropins and melanin concentrating hormone (MCH) as the frog bioassay. 3. On the basis of parallel dose-response curves obtained with the toad skin assay we found that beta-MSH is slightly less active than alpha-MSH, whereas the synthetic analogue [Nle4-D-Phe7]-alpha-MSH is about 10 times more potent and exhibits prolonged biological activity. 4. MCH, a putative neurohormone, can also be bioassayed in the in vitro toad skin bioassay, since it has alpha-MSH-like activity on amphibian melanocytes. 5. Since neither adreno- nor cholinoceptors are present in the toad melanocytes, the assay provides great specificity and sensitivity for the determination of melanotropin activity in tissue or blood.
Assuntos
Hormônios Estimuladores de Melanócitos/farmacocinética , Pele/metabolismo , Animais , Bioensaio , Bufonidae , Masculino , Hormônios Estimuladores de Melanócitos/análise , Pigmentação da Pele/efeitos dos fármacosRESUMO
1. The darkening actions of MCH (melanin concentrating hormone), alpha-MSH and the synthetic analog [Nle4, D-Phe7]-alpha-MSH on the toad, Bufo ictericus ictericus, melanophores were studied regarding the role of calcium in the hormone receptor coupling, signal transduction and intracellular pigment translocation. 2. In the absence of external calcium, MCH and both melanotropins still elicit maximal skin darkening. 3. Verapamil, a calcium-channel blocker, completely abolishes the alpha-MSH-induced response and partially inhibits MCH-induced darkening, although the calcium carrier, ionophore A23187, was unable to promote any pigment translocation. 4. Since darkening responses promoted by cyclic nucleotides proceeded normally in the presence of verapamil and extracellular calcium was not necessary for melanotropin dispersing action, it is suggested that the blocking activity obtained with verapamil is probably due to an impairment of the Ca2+-dependent adenylate cyclase activity. 5. Reversal of melanotropin-induced darkening could be obtained with melatonin, in both normal and Ca2+-free Ringer, whereas MCH darkening is reversed by melatonin only in the absence of calcium. 6. The results seem to indicate that calcium is not required for hormone receptor binding and pigment migration, whereas it is specifically needed for signal transduction.